|Dataset||OMIM Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||An autosomal dominant disease that is characterized by abnormalities affecting the lacrimal and salivary glands and ducts, ears, teeth and fingers and toes. (Human Disease Ontology, DOID_0050331)|
|Downloads & Tools|
3 genes associated with the ladd syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.